A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603953



Internal ID6990984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:8268201..8292227hg38UCSC Ensembl
Innerchr5:8268224..8292204hg38UCSC Ensembl
Outerchr5:8268178..8292250hg38UCSC Ensembl
chr5:8268314..8292340hg19UCSC Ensembl
Innerchr5:8268337..8292317hg19UCSC Ensembl
Outerchr5:8268291..8292363hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3824027
hg1924027
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11805368
SamplesHG02938
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603953
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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